105 related articles for article (PubMed ID: 28358914)
1. Analysis of single nucleotide variants of HFE gene and association to survival in The Cancer Genome Atlas GBM data.
Lee SY; Zhu J; Salzberg AC; Zhang B; Liu DJ; Muscat JE; Langan ST; Connor JR
PLoS One; 2017; 12(3):e0174778. PubMed ID: 28358914
[TBL] [Abstract][Full Text] [Related]
2. Impact of HFE variants and sex in lung cancer.
Lee SY; Walter V; Zhu J; Salzberg AC; Liu DJ; Connor JR
PLoS One; 2019; 14(12):e0226821. PubMed ID: 31856248
[TBL] [Abstract][Full Text] [Related]
3. HFE polymorphisms affect survival of brain tumor patients.
Lee SY; Slagle-Webb B; Sheehan JM; Zhu J; Muscat JE; Glantz M; Connor JR
J Neurooncol; 2015 Mar; 122(1):97-104. PubMed ID: 25491948
[TBL] [Abstract][Full Text] [Related]
4. Prevalence of C282Y, H63D, and S65C mutations in hereditary HFE-hemochromatosis gene in Lithuanian population.
Kucinskas L; Juzenas S; Sventoraityte J; Cedaviciute R; Vitkauskiene A; Kalibatas V; Kondrackiene J; Kupcinskas L
Ann Hematol; 2012 Apr; 91(4):491-5. PubMed ID: 21947086
[TBL] [Abstract][Full Text] [Related]
5. Haemochromatosis HFE gene polymorphisms as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age.
Shi Z; Johnstone D; Talseth-Palmer BA; Evans TJ; Spigelman AD; Groombridge C; Milward EA; Olynyk JK; Suchy J; Kurzawski G; Lubinski J; Scott RJ
Int J Cancer; 2009 Jul; 125(1):78-83. PubMed ID: 19291797
[TBL] [Abstract][Full Text] [Related]
6. Genetic screening for HFE hemochromatosis in 6,020 Danish men: penetrance of C282Y, H63D, and S65C variants.
Pedersen P; Milman N
Ann Hematol; 2009 Aug; 88(8):775-84. PubMed ID: 19159930
[TBL] [Abstract][Full Text] [Related]
7. Hemochromatosis (HFE) and transferrin receptor-1 (TFRC1) genes in sporadic porphyria cutanea tarda (sPCT).
Lamoril J; Andant C; Gouya L; Malonova E; Grandchamp B; Martásek P; Deybac JC; Puy H
Cell Mol Biol (Noisy-le-grand); 2002 Feb; 48(1):33-41. PubMed ID: 11929045
[TBL] [Abstract][Full Text] [Related]
8. HFE p.C282Y homozygosity predisposes to rapid serum ferritin rise after menopause: A genotype-stratified cohort study of hemochromatosis in Australian women.
Warne CD; Zaloumis SG; Bertalli NA; Delatycki MB; Nicoll AJ; McLaren CE; Hopper JL; Giles GG; Anderson GJ; Olynyk JK; Powell LW; Allen KJ; Gurrin LC;
J Gastroenterol Hepatol; 2017 Apr; 32(4):797-802. PubMed ID: 27784128
[TBL] [Abstract][Full Text] [Related]
9. Population-based study of the relationship between mutations in the hemochromatosis (HFE) gene and arthritis.
Sherrington CA; Knuiman MW; Divitini ML; Bartholomew HC; Cullen DJ; Olynyk JK
J Gastroenterol Hepatol; 2006 Mar; 21(3):595-8. PubMed ID: 16638105
[TBL] [Abstract][Full Text] [Related]
10. HFE gene C282Y, H63D and S65C mutations frequency in the Transylvania region, Romania.
Trifa AP; Popp RA; Militaru MS; Farcaş MF; Crişan TO; Gana I; Cucuianu A; Pop IV
J Gastrointestin Liver Dis; 2012 Jun; 21(2):177-80. PubMed ID: 22720307
[TBL] [Abstract][Full Text] [Related]
11. Prevalence of H63D, S65C, and C282Y hereditary hemochromatosis gene variants in Madeira Island (Portugal).
Spínola C; Brehm A; Spínola H
Ann Hematol; 2011 Jan; 90(1):29-32. PubMed ID: 20714725
[TBL] [Abstract][Full Text] [Related]
12. HFE genotype and parameters of iron metabolism in German first-time blood donors - evidence for an increased transferrin saturation in C282Y heterozygotes.
Raddatz D; Legler T; Lynen R; Addicks N; Ramadori G
Z Gastroenterol; 2003 Nov; 41(11):1069-76. PubMed ID: 14648375
[TBL] [Abstract][Full Text] [Related]
13. Hereditary hemochromatosis: mutations in genes involved in iron homeostasis in Brazilian patients.
Santos PC; Cançado RD; Pereira AC; Schettert IT; Soares RA; Pagliusi RA; Hirata RD; Hirata MH; Teixeira AC; Figueiredo MS; Chiattone CS; Krieger JE; Guerra-Shinohara EM
Blood Cells Mol Dis; 2011 Apr; 46(4):302-7. PubMed ID: 21411349
[TBL] [Abstract][Full Text] [Related]
14. [Study on HFE gene mutations in patients with myelodysplastic syndromes and aplastic anemia].
Nie L; Ai XF; Zheng YZ; Li QH; Yang L; Xiao ZJ
Zhonghua Xue Ye Xue Za Zhi; 2009 Apr; 30(4):223-8. PubMed ID: 19731820
[TBL] [Abstract][Full Text] [Related]
15. Frequency of the C282Y and H63D mutations of the hemochromatosis gene (HFE) in 2501 ethnic Danes.
Milman N; Pedersen P; Ovesen L; Melsen GV; Fenger K
Ann Hematol; 2004 Oct; 83(10):654-7. PubMed ID: 15141324
[TBL] [Abstract][Full Text] [Related]
16. A population-based study of the effect of the HFE C282Y and H63D mutations on iron metabolism.
Njajou OT; Houwing-Duistermaat JJ; Osborne RH; Vaessen N; Vergeer J; Heeringa J; Pols HA; Hofman A; van Duijn CM
Eur J Hum Genet; 2003 Mar; 11(3):225-31. PubMed ID: 12673276
[TBL] [Abstract][Full Text] [Related]
17. HFE C282Y homozygosity is associated with lower total and low-density lipoprotein cholesterol: The hemochromatosis and iron overload screening study.
Adams PC; Pankow JS; Barton JC; Acton RT; Leiendecker-Foster C; McLaren GD; Speechley M; Eckfeldt JH
Circ Cardiovasc Genet; 2009 Feb; 2(1):34-7. PubMed ID: 20031565
[TBL] [Abstract][Full Text] [Related]
18. Frequency of the hemochromatosis HFE mutations C282Y, H63D, and S65C in blood donors in the Faroe Islands.
Milman N; á Steig T; Koefoed P; Pedersen P; Fenger K; Nielsen FC
Ann Hematol; 2005 Mar; 84(3):146-9. PubMed ID: 15042317
[TBL] [Abstract][Full Text] [Related]
19. HFE genotype frequencies in consecutive reference laboratory specimens: comparisons among referral sources and association with initial diagnosis.
Acton RT; Barton JC
Genet Test; 2001; 5(4):299-306. PubMed ID: 11960574
[TBL] [Abstract][Full Text] [Related]
20. Prevalence of the C282Y, H63D, and S65C mutations of the HFE gene in 1,146 newborns from a region of Northern Spain.
Altes A; Ruiz A; Barceló MJ; Remacha AF; Puig T; Maya AJ; Castell C; Amate JM; Saz Z; Baiget M
Genet Test; 2004; 8(4):407-10. PubMed ID: 15684872
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]